Arrow recalls specific Pressure Injectable ARROWg+ard Blue PLUS Two-Lumen Central Venous Catheterization Kits due to potential sterility compromise from unsealed packaging. Affected units include lot numbers 13F17D0321, 13F17H0137, 13F:17L0063, and 13F17L0555.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling certain Pressure Injectable ARROWg+ard Blue PLUS Two-Lumen Central Venous Catheterization Kits because the packaging may not be sealed properly, risking contamination. This could lead to infections if the kit is used without proper sterility.
The unsealed packaging could allow contaminants to enter the kit, potentially causing infections if the catheter is used without proper sterility. This is a risk during medical procedures where sterile conditions are critical.
Healthcare professionals who use the recalled catheter kits for central venous line procedures are most at risk. Patients receiving these kits during treatment may also be affected if the kits are used without proper sterility.
Check the product code ASK-42802-PWHC1 on the packaging. Affected units have lot numbers 13F17D0321, 13F17H0137, 13F17L0063, and 13F17L0555.
Look for lot numbers 13F17D0321, 13F17H0137, 13F17L0063, or 13F17L0555 on the packaging.
The packaging may not be sealed properly, which could lead to contamination and infection if the kit is used without proper sterility.
Check the lot numbers on the packaging. If it matches the affected numbers, stop using it and contact Arrow for instructions.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1993-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1993-2018 from Arrow. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
